Recall Z-0768-2025— Jinan Bodor Cnc Machine Co Ltd
Class II · Ongoing
Class II FDA medical device recall by Jinan Bodor Cnc Machine Co Ltd, initiated 2024-12-19. FDA's recall record names no specific 510(k) clearance for this event. Product: Bodor P and C series laser cutting machines. Reason: Non-compliant laser products.
- Recalling firm
- Jinan Bodor Cnc Machine Co Ltd
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-12-19
- Firm location
- Jinan, China
Product description
Bodor P and C series laser cutting machines
Reason for recall
Non-compliant laser products
Data sourced from openFDA. This site is unofficial and independent of the FDA.